Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs279836
rs279836
1 4 46337053 intron variant T/A snv 0.38 0.700 0
dbSNP: rs279845
rs279845
2 1.000 0.080 4 46327706 intron variant T/A snv 0.41 0.700 0
dbSNP: rs279871
rs279871
5 0.882 0.080 4 46303716 intron variant T/C snv 0.38 0.700 0